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Saccharocarcin A

CAS No.
158475-32-2
Chemical Name:
Saccharocarcin A
Synonyms
Saccharocarcin A;18H-16a,19-Metheno-16aH-benzo[b]naphth[2,1-j]oxacyclotetradecin-18,20(1H)-dione, 10-[[4-(acetylamino)-2,4,6-trideoxy-3-C-methylhexopyranosyl]oxy]-4-[[O-2,6-dideoxyhexopyranosyl-(1→4)-O-2,6-dideoxy-3-O-(tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl)hexopyranosyl-(1→4)-2,6-dideoxyhexopyranosyl]oxy]-15-e...
CBNumber:
CB02703761
Molecular Formula:
C67H101NO20
Molecular Weight:
1240.51354
MDL Number:
MOL File:
158475-32-2.mol
Last updated:2023-05-21 10:59:17

Saccharocarcin A Properties

Density 1.30±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMF: Soluble; DMSO: Soluble; Ethanol: Soluble; Methanol: Soluble
form A solid
pka 4.50±1.00(Predicted)

Saccharocarcin A price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 28094 Saccharocarcin A 158475-32-2 500μg $335 2024-03-01 Buy
Cayman Chemical 28094 Saccharocarcin A 158475-32-2 2.5mg $1169 2024-03-01 Buy
Usbiological S0055-10 Saccharocarcin A 158475-32-2 500ug $523 2021-12-16 Buy
AK Scientific 0936EF SaccharocarcinA 158475-32-2 2.5mg $1400 2021-12-16 Buy
Product number Packaging Price Buy
28094 500μg $335 Buy
28094 2.5mg $1169 Buy
S0055-10 500ug $523 Buy
0936EF 2.5mg $1400 Buy

Saccharocarcin A Chemical Properties,Uses,Production

Description

Saccharocarcin A is an antibiotic originally isolated from S. aerocolonigenes subsp. antibiotica. It is active against M. luteus, S. aureus, E. coli, P. aeruginosa, and C. albicans in a disc assay. Saccharocarcin A inhibits C. trachomatis infection by 88% without inducing cytotoxicity in McCoy cells when used at a concentration of 0.5 μg/ml.

Uses

Saccharocarcin A is an unusual tetronic acid structurally related to kijanimicin, chlorothricin, tetrocarcin and versipelostatin, which has pronounced activity against Gram positive bacteria and Chlamydia trachomatis. Limited availability has restricted further investigation of this metabolite, however several members of this class have received considerable literature focus. Versipelostatin inhibits transcription from the promoter of GRP78, a gene that is activated as part of a stress signalling pathway under glucose deprivation resulting in unfolded protein response (UPR), causing death of glucose-deprived cells. Tetrocarcin A appears to target the phosphatidylinositide-3'-kinase/Akt signalling pathway.

Uses

Saccharocarcin A is an unusual tetronic acid with inhibitory effects on gram positive bacteria.

Saccharocarcin A Preparation Products And Raw materials

Raw materials

Preparation Products

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Saccharocarcin A 18H-16a,19-Metheno-16aH-benzo[b]naphth[2,1-j]oxacyclotetradecin-18,20(1H)-dione, 10-[[4-(acetylamino)-2,4,6-trideoxy-3-C-methylhexopyranosyl]oxy]-4-[[O-2,6-dideoxyhexopyranosyl-(1→4)-O-2,6-dideoxy-3-O-(tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl)hexopyranosyl-(1→4)-2,6-dideoxyhexopyranosyl]oxy]-15-e... 158475-32-2